p-Toluenesulfonic acid → HCID 22025475, compound

HRID 1792964Notes

Reaction equation

HRID 1792964 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[O:8][C:6](=O)[C:5]2=[CH:11][CH:12]=1.[CH2:13]([NH2:17])[CH:14]([CH3:16])[CH3:15].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH2:13]([N:17]1[C:9](=[O:10])[C:4]2=[CH:3][C:2]([CH3:1])=[CH:12][CH:11]=[C:5]2[C:6]1=[O:8])[CH:14]([CH3:16])[CH3:15]

Participants

5

Conditions

Temperature
140 °C

Procedure

N-Isobutyl-4-methylphthalimide is prepared as described in Example 2, starting with 6.0 g of 4-methylphthalic anhydride, 3.7 cm3 of isobutylamine and a catalytic amount of para-toluenesulphonic acid in 60 cm3 of toluene. The reaction mixture is heated at a temperature in the region of 140° C. for three hours and is then cooled to a temperature in the region of 20° C. The reaction mixture is concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue is taken up in 50 cm3 of saturated aqueous sodium bicarbonate solution, and the mixture is then extracted twice with 75 cm3 of dichloromethane. The organic extracts are combined, dried over sodium sulphate, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 30° C., giving 6.7 g of N-isobutyl-4-methylphthalimide in the form of a white solid melting at 102° C.

Workup

  1. customN-Isobutyl-4-methylphthalimide is prepared
  2. temperatureis then cooled to a temperature in the region of 20° C
  3. concentrationThe reaction mixture is concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C
  4. extractionthe mixture is then extracted twice with 75 cm3 of dichloromethane
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 30° C.

Sources & evidence

ORD record
ord-8d0acc1108a0435e9315b9e987106bc9
Source dataset
uspto-grants-2006_07
Patent number
US07078428B2

Reaction notes

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